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Kinetics of dissociative water adsorption on stepped Si(001), on Si(115), Si(113), Si(5,5,12) and Si(112)

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Ranke,  Wolfgang
Fritz Haber Institute, Max Planck Society;

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Citation

Ranke, W., & Xing, Y. (1997). Kinetics of dissociative water adsorption on stepped Si(001), on Si(115), Si(113), Si(5,5,12) and Si(112). Surface Science, 381(1), 1-11. doi:10.1016/S0039-6028(97)00064-2.


Cite as: https://hdl.handle.net/21.11116/0000-0008-B4C1-2
Abstract
We present photoelectron spectroscopic and low energy electron diffraction measurements of water adsorption on flat Si samples of the orientations (001), (115), (113), (5,5,12) and (112) as well as on curved samples covering continuously the ranges (001)-(117) and (113)-(5,5,12)-(112). On all orientations, water adsorption is dissociative (OH and H) and non-destructive. On Si(001) the sticking coefficient S and the saturation coverage Θsat are largest. On Si(001) and for small miscuts in the [110]-azimuth, S is constant nearly up to saturation which proves that the kinetics involves a weakly bound mobile precursor state. For (001)-vicinals with high miscut angles (9–13°), the step structure breaks down, the precursor mobility is affected and the adsorption kinetics changed. On (115), (113), (5,5,12) and (112), the values of S and Θsat are smaller which indicates that not all sites are able to dissociate and bind water. For (113) the shape of the adsorption curves Θ versus exposure shows the existence of two adsorption processes, one with mobile precusor kinetics and one with Langmuir-like kinetics. On (5,5,12), two processes with mobile precursor kinetics are observed which are ascribed to adsorption on different surface regions within the large surface unit cell. From the corresponding values of S and Θsat, data for structure models are deduced.